KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy - Li, Ning; Xu, Ying-Jia; Shi, Hong-Yu; Yang, Chen-Xi; Guo, Yu-Han; Li, Ruo-Gu; Qiu, Xing-Biao; Yang, Yi-Qing; Zhang, Min (Genes, 2021)
Keywords: Arrhythmia; atrial fibrillation; Binding sites; bioinformatics; Cardiac arrhythmia; Cardiomyopathy; Cardiovascular disease; Congestive heart failure; Connective tissue growth factor; death; Deoxyribonucleic acid; DNA; DNA polymerase; Electrocardiography; Electrophysiology; Enzymes; Fibrillation; Gene expression; genes; genetic heterogeneity; Genomes; Growth factors; Heart; heart failure; heterozygosity; Hospitals; Laboratories; loss-of-function mutation; Molecular modelling; Mutagenesis; mutants; Mutation; pathogenesis; pedigree; penetrance; Plasmids; Polymorphism; Potassium channels (voltage-gated); stroke; transcription (genetics); Transcription activation; transcription factors; transcriptional activation; Transforming growth factor-b1; Ventricle; United States--US; transcription factor; atrial fibrillation; genetics; cardiomyopathy; KLF15; arrhythmia